MY-SHIELD HAND SANITIZER GEL- benzalkonium chloride gel

My-Shield Hand Sanitizer Gel by

Drug Labeling and Warnings

My-Shield Hand Sanitizer Gel by is a Otc medication manufactured, distributed, or labeled by Enviro Specialty Chemicals Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient: 

Benzalkonium Chloride 0.13%

Purpose:

Antiseptic/Hand & Skin Sanitizer

Uses:

Hand Sanitizer to help decrease bacteria on the skin - Recommended for repeated use.

Warnings:

Do not freeze. For external use only.

Do not use in ears, eyes or mouth.

When using this product, avoid contact with the eyes. In case of contact, flush eyes with water.

Stop use and ask a doctor if redness or irritation develops and persists for more than 72 hours.

Children should be supervised when using this product.

Keep out of reach of children.

Directions:

Apply liberally to the palms of the hands. Rub into skin until dry. Recommended for repeat use

Inactive Ingredients:

Aloe Barbadensis leaf extract, Aqua, Citric Acid, Caprylyl Glucoside, Hydroxyethyl Cellulose,

Polyhexanide, Phenoxyethanol, Triethoxysilylpropyl Steardimonium Chloride.

Questions?

+1(888) 331-8332, M-F, 9AM-5PM (EST)

SPL UNCLASSIFIED SECTION

FAST ACTING 15 SECOND FORMULA

WITH SOOTHING ALOE VERA

Long lasting, alcohol-free protection from germs for your hands.

KILLS 99.99% OF GERMS

Formulated and enhanced with Zetrisil

FORMULATED IN THE USA

MADE IN CHINA

DISTRIBUTED BY ESC BRANDS, LLC.

664 OLD HARGRAVES ROAD - SUITE B

LEXINGTON, NC 27295

www.myshield.com

Packaging

INGREDIENTS AND APPEARANCE

MY-SHIELD HAND SANITIZER GEL 
benzalkonium chloride gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71884-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)
HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
POLIHEXANIDE (UNII: 322U039GMF)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDE (UNII: XGN40YQC7B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71884-011-01	3 in 1 PACKAGE	05/26/2020
1		30 mL in 1 TUBE; Type 0: Not a Combination Product
2	NDC: 71884-011-02	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/26/2020
3	NDC: 71884-011-04	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/26/2020
4	NDC: 71884-011-06	177 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/26/2020
5	NDC: 71884-011-08	244 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/26/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	05/26/2020

Labeler - Enviro Specialty Chemicals Inc (202621850)